
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
FGF-7 CRISPR/Cas9 KO Plasmid (h) | sc-401243 | 20 µg | $397.00 |
FGF7 encodes fibroblast growth factor 7 (FGF-7, also known as keratinocyte growth factor), a paracrine ligand produced largely by mesenchymal cells that signals primarily through FGFR2b on epithelial targets. This signaling axis regulates epithelial proliferation, migration, and differentiation and contributes to tissue repair and barrier maintenance through downstream MAPK/ERK, PI3K/AKT, and related growth-factor pathways. Dysregulated FGF7–FGFR2b signaling has been implicated in epithelial hyperplasia, fibrosis-associated remodeling, and tumor–stroma interactions that influence carcinoma growth and invasion. As a model factor in epithelial–mesenchymal crosstalk, FGF-7 is frequently studied in contexts such as wound-healing biology, airway and gastrointestinal epithelium homeostasis, and microenvironment-driven signaling.
FGF-7 CRISPR/Cas9 KO Plasmid (h) is a pool of plasmids designed for targeted disruption of the FGF7 gene in human cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the FGF7 together with the Streptococcus pyogenes Cas9 nuclease. The plasmids also encode GFP, allowing fluorescent identification and enrichment of successfully transfected cells by fluorescence microscopy or flow cytometry.
The multi-guide design increases the likelihood of generating insertions or deletions (indels) that disrupt the FGF7 open reading frame following Cas9-mediated double-strand break formation. DNA breaks introduced by the CRISPR/Cas9 system are repaired through endogenous non-homologous end joining (NHEJ) pathways, frequently resulting in frameshift mutations that abolish FGF-7 protein expression.
This CRISPR knockout system enables efficient generation of FGF7-deficient cell models for investigation of FGF-7 signaling, functional genomics studies, cancer biology research, and evaluation of therapeutic responses in human cell lines.
CRISPRs +/- HDRs
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.